Simple preparation of carbon-bimetal oxide nanospinels for high-performance bifunctional oxygen electrocatalysts

被引:8
|
作者
Malaie, Keyvan [1 ]
Jeyabharathi, Chinnaiah [2 ]
Wulff, Harm [3 ]
Ganjali, Mohammad Reza [1 ]
Soavi, Francesca [4 ]
Scholz, Fritz [2 ]
机构
[1] Univ Tehran, Sch Chem, Ctr Excellence Electrochem, Coll Sci, Enghelab St, Tehran 1417614411, Iran
[2] Ernst Moritz Arndt Univ Greifswald, Inst Biochem, Felix Hausdorff Str 4, D-17487 Greifswald, Germany
[3] Ernst Moritz Arndt Univ Greifswald, Inst Phys, Felix Hausdorff Str 4, D-17487 Greifswald, Germany
[4] Alma Mater Studiorum Univ Bologna, Dept Chem Giacomo Ciamician, Via Selmi 2, I-40126 Bologna, Italy
关键词
WATER OXIDATION; EFFICIENT ELECTROCATALYSTS; CATALYTIC-ACTIVITY; HYDROGEN-PEROXIDE; FACILE SYNTHESIS; RATIONAL DESIGN; EVOLUTION; NANOPARTICLES; NI; CO;
D O I
10.1039/c8nj04566f
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The lack of efficient cost-effective electrocatalysts for reversible oxidation of water is by far the most notorious obstacle in the development of fuel cells and electrolyzers. Here, oxygen bifunctional electrocatalysts based on C-CoFe and C-NiFe oxide nanospinels are developed by simple autocombustion between ethylene glycol/acetate and the metal nitrates. The effects of electronic modulation and the mass (or surface area) effect were examined based on the cyclic voltammograms of the unary and binary metal oxides in alkaline solution, and their high oxygen evolution and reduction activities were attributed to the synergic intermetallic interactions. The C-CoFe oxide, in particular, shows an oxygen evolution overpotential of 350 mV (without iR correction) at 10 mA cm(-2) with excellent stability over 10 hours and a Tafel slope of 49 mV per decade. Furthermore, it exhibits the highest oxygen reduction activity among the synthesized electrocatalysts due the particular synergy between Co and Fe centers.
引用
收藏
页码:20156 / 20162
页数:7
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